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Main
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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register. |
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Register:
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ClinicalTrials.gov |
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Last refreshed on:
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9 May 2016 |
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Main ID: |
NCT02751970 |
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Date of registration:
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21/04/2016 |
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Prospective Registration:
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No |
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Primary sponsor: |
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Public title:
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Clinical Trial of the Effect of Different Categories of Adhesive System
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Scientific title:
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Randomized Clinical Trial of the Effect of Different Categories of Adhesive System |
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Date of first enrolment:
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April 2014 |
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Target sample size:
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185 |
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Recruitment status: |
Active, not recruiting |
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URL:
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https://clinicaltrials.gov/show/NCT02751970 |
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Study type:
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Interventional |
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Study design:
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Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Outcomes Assessor), Primary Purpose: Treatment
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Phase:
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Phase 2
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Countries of recruitment
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Chile
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Contacts
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Name:
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Issis Luque, professor |
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Address:
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Telephone:
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Email:
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Affiliation:
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Pontificia Universidad Catolica de Chile |
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Key inclusion & exclusion criteria
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Inclusion Criteria:
- Good general health,
- Patients with acceptable oral hygiene level,
- Patients with at least 20 teeth under occlusion.
- Patients with at least four non-carious cervical lesions in four different teeth
- Patients with maximum of eight lesions that needed to be restored.
- These lesions had to be non-carious, non-retentive, deeper than 1 mm, and involve
both the enamel and dentin of vital teeth without mobility.
Exclusion Criteria:
- Patients with extremely poor oral hygiene,
- Patients with severe or chronic periodontitis,
- Patients with heavy bruxism habits.
Age minimum:
18 Years
Age maximum:
N/A
Gender:
Both
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Health Condition(s) or Problem(s) studied
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Dental Caries
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Intervention(s)
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Procedure: 1 step SE
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Procedure: 3 step ER
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Procedure: 2 step ER
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Procedure: 2 step SE
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Procedure: Dental restoration
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Primary Outcome(s)
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Retention rate
[Time Frame: one year]
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Secondary caries
[Time Frame: one year]
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Secondary Outcome(s)
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Marginal discoloration
[Time Frame: one year]
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Marginal integrity
[Time Frame: one year]
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post-operative sensitivity
[Time Frame: one year]
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Secondary ID(s)
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CB027-2014
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Source(s) of Monetary Support
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Please refer to primary and secondary sponsors
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Results
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Results available:
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Date Posted:
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Date Completed:
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URL:
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